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The NADPH Oxidase Nox4 and Aging in the Heart
Oxidative stress in mitochondria is believed to promote aging. Although passive leakage of electron from the mitochondrial electron transport chain has been considered as a major source of oxidative stress in the heart and the cardiomyocytes therein, enzymes actively producing reactive oxygen specie...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3034169/ https://www.ncbi.nlm.nih.gov/pubmed/21212466 |
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author | Ago, Tetsuro Matsushima, Shouji Kuroda, Junya Zablocki, Daniela Kitazono, Takanari Sadoshima, Junichi |
author_facet | Ago, Tetsuro Matsushima, Shouji Kuroda, Junya Zablocki, Daniela Kitazono, Takanari Sadoshima, Junichi |
author_sort | Ago, Tetsuro |
collection | PubMed |
description | Oxidative stress in mitochondria is believed to promote aging. Although passive leakage of electron from the mitochondrial electron transport chain has been considered as a major source of oxidative stress in the heart and the cardiomyocytes therein, enzymes actively producing reactive oxygen species may also exist in mitochondria. We have shown recently that Nox4, a member of the NADPH oxidase family, is localized on intracellular membranes, primarily at mitochondria, in cardiomyocytes. Mitochondrial expression of Nox4 is upregulated by cardiac stress and aging in the heart, where Nox4 could become a major source of oxidative stress. This raises an intriguing possibility that Nox4 may play an important role in mediating aging of the heart. Here we discuss the potential involvement of Nox4 in mitochondrial oxidative stress and aging in the heart. |
format | Text |
id | pubmed-3034169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-30341692011-02-08 The NADPH Oxidase Nox4 and Aging in the Heart Ago, Tetsuro Matsushima, Shouji Kuroda, Junya Zablocki, Daniela Kitazono, Takanari Sadoshima, Junichi Aging (Albany NY) Research Perspective Oxidative stress in mitochondria is believed to promote aging. Although passive leakage of electron from the mitochondrial electron transport chain has been considered as a major source of oxidative stress in the heart and the cardiomyocytes therein, enzymes actively producing reactive oxygen species may also exist in mitochondria. We have shown recently that Nox4, a member of the NADPH oxidase family, is localized on intracellular membranes, primarily at mitochondria, in cardiomyocytes. Mitochondrial expression of Nox4 is upregulated by cardiac stress and aging in the heart, where Nox4 could become a major source of oxidative stress. This raises an intriguing possibility that Nox4 may play an important role in mediating aging of the heart. Here we discuss the potential involvement of Nox4 in mitochondrial oxidative stress and aging in the heart. Impact Journals LLC 2010-12-27 /pmc/articles/PMC3034169/ /pubmed/21212466 Text en Copyright: © 2010 Ago et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Perspective Ago, Tetsuro Matsushima, Shouji Kuroda, Junya Zablocki, Daniela Kitazono, Takanari Sadoshima, Junichi The NADPH Oxidase Nox4 and Aging in the Heart |
title | The NADPH Oxidase Nox4 and Aging in the Heart |
title_full | The NADPH Oxidase Nox4 and Aging in the Heart |
title_fullStr | The NADPH Oxidase Nox4 and Aging in the Heart |
title_full_unstemmed | The NADPH Oxidase Nox4 and Aging in the Heart |
title_short | The NADPH Oxidase Nox4 and Aging in the Heart |
title_sort | nadph oxidase nox4 and aging in the heart |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3034169/ https://www.ncbi.nlm.nih.gov/pubmed/21212466 |
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